从印度分离到的产青霉素 V 的青霉 rubens 菌株 BIONCL P45 的基因组测序和分析。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-10-01 Epub Date: 2024-02-22 DOI:10.1007/s10123-024-00491-0
Amol M Sawant, Vishwambar D Navale, Koteswara Rao Vamkudoth
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引用次数: 0

摘要

背景:丝状真菌鲁本青霉(Penicillium rubens)被广泛认为可以在工业规模上生产重要的抗生素--青霉素:为了更好地理解野生型红青霉菌的遗传蓝图,我们从印度分离了红青霉菌,以确定苯氧甲基青霉素(青霉素 V,PenV)和其他次级代谢产物的遗传/生物合成途径:方法:分离基因组 DNA(gDNA),并按照 Illumina 平台制备文库。根据 Illumina NovoSeq 平台进行全基因组测序(WGS)。此外,还使用 SOAPdenovo 对经 Bowtie-2 和 SAMtools 软件包验证的短读数进行组装。Glimmer 和 GeneMark 用于挖掘基因组中的总基因。预测蛋白质的功能注释由 NCBI 非冗余(NR)、UniProt、京都基因组百科全书(KEGG)和基因本体(GO)数据库完成。此外,还利用 SignalP 4.1 和 TargetP v1.1 进行了分泌组分析,利用 CAZy 数据库进行了碳水化合物活性酶(CAZymes)和蛋白酶家族分析。用 Mauve 2.4.0. 软件进行了比较基因组分析,发现了红青霉菌 BIONCL P45 与干青霉 Wisconsin 54-1255 之间的基因组相关性;还用 ParSNP 工具与已知的青霉素生产菌株进行了系统进化分析:结果:从印度分离出了红青霉 BIONCL P45 菌株,它能产生过量的 PenV。该菌株的基因组为 31.09 Mb,参考基因组 P. chrysogenum Wis 54-1255 的覆盖率为 95.6%,共有 10687 个蛋白质编码基因,其中 3502 个基因在 NR、UniProt、KEGG 和 GO 数据库中有同源物。此外,基因组中还发现了 358 个 CAZymes 和 911 个转运体编码基因。基因组中包含青霉素、苯乙酸(PAA)分解代谢的同戊酸途径、Andrastin A、Sorbicillin、Roquefortine C 和 Meleagrin 的完整途径。BIONCL P45 和 Wis 54-1255 的比较基因组分析显示,其基因组覆盖率为 99.89%,有 2952 个共同的 KEGG 同源蛋白编码基因。系统发生分析表明,BIONCL P45 与弗莱明的原始分离物 P. rubens IMI 15378 聚类:结论:该基因组可为进一步研究开发高滴度青霉素生产的发酵工艺和菌株工程方法提供有用的资源。
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Genome sequencing and analysis of penicillin V producing Penicillium rubens strain BIONCL P45 isolated from India.

Background: A filamentous fungus Penicillium rubens is widely recognized for producing industrially important antibiotic, penicillin at industrial scale.

Objective: To better comprehend, the genetic blueprint of the wild-type P. rubens was isolated from India to identify the genetic/biosynthetic pathways for phenoxymethylpenicillin (penicillin V, PenV) and other secondary metabolites.

Method: Genomic DNA (gDNA) was isolated, and library was prepared as per Illumina platform. Whole genome sequencing (WGS) was performed according to Illumina NovoSeq platform. Further, SOAPdenovo was used to assemble the short reads validated by Bowtie-2 and SAMtools packages. Glimmer and GeneMark were used to dig out total genes in genome. Functional annotation of predicted proteins was performed by NCBI non-redundant (NR), UniProt, Kyoto Encyclopedia of Genes and Genomes (KEGG), and Gene Ontology (GO) databases. Moreover, secretome analysis was performed by SignalP 4.1 and TargetP v1.1 and carbohydrate-active enzymes (CAZymes) and protease families by CAZy database. Comparative genome analysis was performed by Mauve 2.4.0. software to find genomic correlation between P. rubens BIONCL P45 and Penicillium chrysogenum Wisconsin 54-1255; also phylogeny was prepared with known penicillin producing strains by ParSNP tool.

Results: Penicillium rubens BIONCL P45 strain was isolated from India and is producing excess PenV. The 31.09 Mb genome was assembled with 95.6% coverage of the reference genome P. chrysogenum Wis 54-1255 with 10687 protein coding genes, 3502 genes had homologs in NR, UniProt, KEGG, and GO databases. Additionally, 358 CAZymes and 911 transporter coding genes were found in genome. Genome contains complete pathways for penicillin, homogentisate pathway of phenyl acetic acid (PAA) catabolism, Andrastin A, Sorbicillin, Roquefortine C, and Meleagrin. Comparative genome analysis of BIONCL P45 and Wis 54-1255 revealed 99.89% coverage with 2952 common KEGG orthologous protein-coding genes. Phylogenetic analysis revealed that BIONCL P45 was clustered with Fleming's original isolate P. rubens IMI 15378.

Conclusion: This genome can be a helpful resource for further research in developing fermentation processes and strain engineering approaches for high titer penicillin production.

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ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
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